Search

Continuous measurements of particle number size distributions in the size range from 10 nm to 800 nm were performed from 2015 to 2019 at the ECO Environmental-Climate Observatory of Lecce (Global Atmosphere Watch Programme/Aerosol, Clouds and Trace Gases Research Infrastructure (GAW/ACTRIS) regional station). The main objectives of this work were to investigate the daily, weekly and seasonal trends of particle number concentrations and their dependence on meteorological parameters gathering information on potential sources. The highest total number concentrations were observed during autumn-winter with average values nearly twice as high as in summer. More than 52% of total particle number concentration consisted of Aitken mode (20 nm < particle diameter (Dp) < 100 nm) particles followed by accumulation (100 nm < Dp < 800 nm) and nucleation (10 nm < Dp < 20 nm) modes representing, respectively, 27% and 21% of particles. The total number concentration was usually significantly higher during workdays than during weekends/holidays in all years, showing a trend likely correlated with local traffic activities. The number concentration of each particle mode showed a characteristic daily variation that was different in cold and warm seasons. The highest concentrations of the Aitken and accumulation particle mode were observed in the morning and the late evening, during typical rush hour traffic times, highlighting that the two-particle size ranges are related, although there was significant variation in the number concentrations. The peak in the number concentrations of the nucleation mode observed in the midday of spring and summer can be attributed to the intensive formation of new particles from gaseous precursors. Based on Pearson coefficients between particle number concentrations and meteorological parameters, temperature, and wind speed had significant negative relationships with the Aitken and accumulation particle number concentrations, whereas relative humidity was positively correlated. No significant correlations were found for the nucleation particle number concentrations.

In this paper an analysis of different indirect methods for the calculation of the boundary layer height (BLH) using sodar, ultrasonic anemometer and a prognostic model based on single point surface measurements is presented. In particular the automatic spectral routine developed for Remtech sodar is compared with the results obtained with the parameterization of the vertical velocity variance of a minisodar, with the calculation of a prognostic model, with a parameterization based on horizontal velocity spectra and with the BLH evaluated from the intensity of minisodar echoes in stable conditions. The data of a radiosonde system taken in a nearby site was also analysed to get an independent evaluation of BLH for comparison. There is a significant scatter in the data for both the evaluation through the variance of vertical wind speed and the spectral analysis of the horizontal wind velocity although created by different effects. In unstable conditions the different methods give a similar pattern even if the prognostic model in some days predicts a significantly higher BLH with respect to the other methods. In stable nocturnal conditions the performances of the Remtech routine are worse than those in unstable conditions with an evident overestimation of the BLH that it is likely related to the overestimation of vertical turbulence and to the use of multiple range gates in the algorithm. Taking as reference the evaluation of BLH of the sodar, the spectral method applied to ultrasonic anemometer data seems to be affected by the lowest biases and it is a possible candidate, for the development of automatic routines for operational evaluation of BLH possibly with a different parameterisation for stable and unstable cases.

An approach based on the Penman-Monteith equation was used to estimate the actual evapotranspiration from local meteorological data over non-homogeneous land cover in a Mediterranean site in the south-east of Italy, with two six month data sets from two different years of measurements (2006 and 2009). The "critical resistance" formulation was used in different forms to model the surface resistance, together with some modifications to take into account the soil moisture content. One, two, or three model parameters were estimated, one of them related to the atmospheric resistance and the others to the surface resistance, and the calibration was made by either linear regression or nonlinear minimization of a proper cost function, depending on the applicability. Two kinds of cost functions were tested, the first depending on both the latent heat flux and the difference between screen air temperature and surface radiometric temperature, and the second depending on the temperature difference only. In all cases the calculated fluxes give better results with respect to both a flux-gradient approach and a complementarity based method, that require comparable data inputs. However the calibration by the temperature differences only, that requires no turbulent flux measurements, considerably increases the statistical uncertainty of the calibration parameters. The inclusion of the soil moisture did not significantly improve the model results in the considered site. [ABSTRACT FROM AUTHOR]

Continuous measurements of particle number size distributions in the size range from 10 nm to 800 nm were performed from 2015 to 2019 at the ECO Environmental-Climate Observatory of Lecce (Global Atmosphere Watch Programme/Aerosol, Clouds and Trace Gases Research Infrastructure (GAW/ACTRIS) regional station). The main objectives of this work were to investigate the daily, weekly and seasonal trends of particle number concentrations and their dependence on meteorological parameters gathering information on potential sources. The highest total number concentrations were observed during autumn-winter with average values nearly twice as high as in summer. More than 52% of total particle number concentration consisted of Aitken mode (20 nm < particle diameter (Dp) < 100 nm) particles followed by accumulation (100 nm < Dp < 800 nm) and nucleation (10 nm < Dp < 20 nm) modes representing, respectively, 27% and 21% of particles. The total number concentration was usually significantly higher during workdays than during weekends/holidays in all years, showing a trend likely correlated with local traffic activities. The number concentration of each particle mode showed a characteristic daily variation that was different in cold and warm seasons. The highest concentrations of the Aitken and accumulation particle mode were observed in the morning and the late evening, during typical rush hour traffic times, highlighting that the two-particle size ranges are related, although there was significant variation in the number concentrations. The peak in the number concentrations of the nucleation mode observed in the midday of spring and summer can be attributed to the intensive formation of new particles from gaseous precursors. Based on Pearson coefficients between particle number concentrations and meteorological parameters, temperature, and wind speed had significant negative relationships with the Aitken and accumulation particle number concentrations, whereas relative humidity was positively correlated. No significant correlations were found for the nucleation particle number concentrations. [ABSTRACT FROM AUTHOR]

In this work, results of scattering and backscattering coefficients, scattering Ångström exponent (SAE), single scattering albedo (SSA), and asymmetry parameter (g) of atmospheric aerosols are presented. All these parameters were measured during the month of April 2016 in Southern Italy on three different Global Atmosphere Watch observatories in the Central Mediterranean. This is the first time, to our knowledge, that optical aerosol properties were studied at the same time, even if in a brief intensive measurement campaign, at three sites in the South of Italy. In order to obtain a characteristic value for aerosol optical properties, different kinds of particle sources (i.e., dust, marine, and anthropic) have been identified and studied. In the measurement period, one event of a long-range transport of Saharan dust from Northern Africa was observed at all observatories. During the Saharan dust transport event, a minimum value of the SAE (0.69 ± 0.34) and a relatively higher values of SSA were observed. During the dust event, g increased up to 0.69. Marine aerosol contribution and anthropic/urban aerosol intrusion were analysed. From this analysis, SAE average values were 0.70, 0.84, and 1.22, respectively, for dust, marine, and anthropic particles. On the other hand, the SSA minimum value was 0.86 for anthropic particles, and it increased for dust (0.88) and marine (0.93) aerosols. The asymmetry parameter had a limited variability for the three types of aerosol from 0.62 to 0.58, as reported also in literature. [ABSTRACT FROM AUTHOR]